DFBP ID - DFBPAMIC0282(Antimicrobial peptide)

DFBP ID DFBPAMIC0282 Peptide sequence VYQHQKAMKPWIQPKTKVIPYVRY Type Native peptide Peptide/Function name Antimicrobial peptide, f(183-206) of bovine alpha s2-casein

Function-activity relationship

Main bioactivity Antimicrobial activity Otheir bioactivity Mineral-binding activity [D1], Haemolytic activity [D2], Multifunctional activity [D3]

Calculated physicochemical properties

Three-letter amino acid Val-Tyr-Gln-His-Gln-Lys-Ala-Met-Lys-Pro-Trp-Ile-Gln-Pro-Lys-Thr-Lys-Val-Ile-Pro-Tyr-Val-Arg-Tyr Single-letter amino acid VYQHQKAMKPWIQPKTKVIPYVRY Peptide length 24 Peptide mass Experimental mass Theoretical mass N.D 3002.62 Da c Net charge 0.00 c Isoelectric point (pI) 10.48 c IC50 N.D pIC50 N.D GRAVY -0.7833 c Hydrophilic residue ratio 45.83% c Peptide calculator To calculate the physicochemical properties of bioactive peptide.

Peptide source & Food-borne protein(s) search

Classification Animal Organism/Source Bovine Precursor protein αs2-Casein Residue position f(183-206) Precursor protein(s) search Source.1: DFBPPR8494 ---- Milk proteins ---- Alpha-S2-casein Link-research Inductive analysis There are no literature reports on the discovery of this sequence in other food-source proteins.

Biological/Functional activity & target protein

Antimicrobial activity Antimicrobial activity Specific target protein(s) N.D

Taste properties & Structure

Bitterness Literature report N.D Bitter prediction tools Bitter taste prediction SMILES N[C@@]([H])(C(C)C)C(=O)N[C@@]([H])(Cc1ccc(O)cc1)C(=O)N[C@@]([H])(CCC(=O)N)C(=O)N[C@@]([H])(CC1=CN=C-N1)C(=O)N[C@@]([H])(CCC(=O)N)C(=O)N[C@@]([H])(CCCCN)C(=O)N[C@@]([H])(C)C(=O)N[C@@]([H])(CCSC)C(=O)N[C@@]([H])(CCCCN)C(=O)N1[C@@]([H])(CCC1)C(=O)N[C@@]([H])(CC(=CN2)C1=C2C=CC=C1)C(=O)N[C@@]([H])([C@]([H])(CC)C)C(=O)N[C@@]([H])(CCC(=O)N)C(=O)N1[C@@]([H])(CCC1)C(=O)N[C@@]([H])(CCCCN)C(=O)N[C@@]([H])([C@]([H])(O)C)C(=O)N[C@@]([H])(CCCCN)C(=O)N[C@@]([H])(C(C)C)C(=O)N[C@@]([H])([C@]([H])(CC)C)C(=O)N1[C@@]([H])(CCC1)C(=O)N[C@@]([H])(Cc1ccc(O)cc1)C(=O)N[C@@]([H])(C(C)C)C(=O)N[C@@]([H])(CCCNC(=N)N)C(=O)N[C@@]([H])(Cc1ccc(O)cc1)C(=O)O

Preparation method

Mode of preparation Synthesis Enzyme(s)/starter culture No enzyme

Stability & Cytotoxicity

Peptide stability Literature report: N.D EHP-Tool: Enzymatic Hydrolysis Prediction Tool (EHP-Tool) Peptide cytotoxicity Literature report: N.D Prediction: ToxinPred

Additional information

Additional information N.D

Database cross-references

DFBP [D1] DFBPMIBP0019 [D2] DFBPHAPE0020 [D3] DFBPMUFU0706

BIOPEP-UWM [D4] 3033, 3435, 3965

APD [D5] -

BioPepDB [D6] -

MBPDB [D7] -

Reference(s)

Primary literature Production of antibacterial peptides from biological fluids. Abstracts of Communications of the European Dairy Experts Symposium, Arnhem, 65 Other literature(s) N.D PubDate 1998